Conclusion the drug release mainly depends on the gel erosion.
结论药物释放主要取决于凝胶溶蚀。
The materials are suitable for making soft contact lens and drug release matrix.
用本法合成的材料是制作较接触镜及药物慢释放基质的理想材料。
Taking Ib as a model drug, the drug release behaviors of the capsules were studied.
以布洛芬为模型药物，初步研究了微囊载体的缓释行为。
OBJECTIVE To predict drug release from the extended formulations by grey maths model.
目的运用灰色数学理论预测长效缓释蛋白微球的体外释药过程。
This study focuses on mathematical modeling of drug release from PLGA cylindrical millirods.
这项研究集中在药物从PLGA圆筒型微囊中释放的数学模型。
Methods the influencing factors on the drug release were investigated by use of similarity factor method.
方法采用相似因子法考察影响药物释放速率的因素，并考察了其释药机理。
Objective To prepare aciclovir sustained-release pellets and investigate the drug release mechanism in vitro.
目的制备阿昔洛韦缓释微丸，并对其体外释药情况进行研究。
Results the gel erosion and drug release were increased with the increase of surface area and shaking frequency.
结果凝胶溶蚀和药物释放随着振荡频率和释放面积的增加而加快。
The results showed that the drug release from MTX liposomes was in conformity with the first-order dynamic equation.
结果表明：甲氨喋呤脂质体的药物释放速率符合一级动力学方程。
Objective To study the preparation technique and in vitro drug release of adriamycin gelatin microspheres (ADM-GMS).
目的对阿霉素明胶微球（ADM-GMS）的制备工艺及体外释药特性进行研究。
Methods Coating prescription was optimized by uniform design and the drug release characteristic was tested in vitro.
方法采用均匀设计优化包衣处方，对度米芬渗透泵片进行体外释放度试验。
OBJECTIVE To prepare sustained-release Hippophae rhamnoides(TFH) tablet and evaluate the rule of drug release property.
目的评价醋柳黄酮缓释片的缓释效果并考察其体外释放规律。
OBJECTIVE To study the preparation process, assay and in vitro drug release of adriamycin polylactic acid microspheres.
目的：对阿霉素聚乳酸微球的制备工艺、含量测定及体外释药特性进行初步研究。
The results showed that the lag time before drug release was lengthened with the increase of the viscosity grade of HPMC.
结果表明，HPMC粘度增加使药物释放滞后时间延长，但高粘度HPMC会导致药物释放无明显突跃点；
Aim to prepare the micelles of stearic acid grafted chitosan oligosaccharide and investigate the drug release from micelles.
目的考察阳离子型壳寡糖硬脂酸嫁接物胶团的理化性质及载药胶团的体外药物释放。
The injectable hydrogel for its unique phase transition behavior is expected to be widely used in the field of drug release.
其中，可注射水凝胶因其独特的溶胶-凝胶相转变性质，在药物控制释放领域有着广泛应用。
The USES of biodegradable polymers poly-asparagine and its derivatives, as carriers in controlled drug release are reviewed.
综述了可生物降解的高分子材料聚天各酰胺及其衍生物作为载体在药物控制释放中的应用。
A few of evaluation methods for drug release in vitro of sustained-controlled matrix tablets were introduced in this review.
本文简要介绍了几种缓控释骨架片药物体外释放行为的评价方法。
Aim To prepare ondansetron hydrochloride osmotic pump tablets (OND-OPT) and investigate their in vitro drug release behavior.
目的制备盐酸昂丹司琼渗透泵型控释片剂(OND - OPT)并考察体外释药特性。
OBJECTIVE To evaluate drug release properties in vitro of the hydrogel films made of cross-linked hyaluronic acid derivatives.
目的对交联透明质酸衍生物制备的载药水凝胶膜进行体外药物释放研究。
A mathematical model describing the drug release from porous polymer was established by using the species continuity equation.
以组分的连续性方程为基础，建立了药物从多孔骨架聚合物系统中释放的数学模型。
The formalation design for oral DDS or GIDS is essential to achieveprolonging stomach residence time and improving drug release.
经口给药的DDS大多以延长药剂在胃内滞留时间和改善药物释放为其设计出发声点。
CONCLUSION The TFH tablet has sustained release property in vitro. The drug release pattern is in accord with Weibull distribution.
结论醋柳黄酮缓释片缓释效果显著，体外释放符合威布尔分布模型。
Aim To prepare Clarithromycin floating beads and investigate its buoyancy, entrapment efficiency and drug release behavior in vitro.
目的制备克拉霉素胃漂浮小丸，考察其漂浮性，包封率和体外释药行为。
The efficiency of drug release in this study has also confirmed that one single dose a day is most likely enough in treating the virus.
在本次研究中对药物释放效率的考察表明每日给药一次足够用于对病毒的治疗。
OBJECTIVE:To study the factor of influencing drug release from diclofenac sodium(DS)tablet coated with ethylcellulose aqueous dispersion.
目的：考察影响双氯芬酸钠乙基纤维素水性分散体包衣片体外释药的因素。
Drug release rate was significantly influenced by release area, stirring speed of peddles and the sorts of dispersion mediums respectively.
释放面积，桨的搅拌速度及释放介质均影响脂质体凝胶的溶蚀及药物的释放。
Conclusion: Oscillating magnetic fields could promote drug release of SPCPGM repeatedly and the release of this system lasted more than 3 weeks.
结论：SPCPGM具有药物缓释功能，振荡磁场可重复性增加体系中药物的溶出，此体系药物缓释周期超过3周。
Methods The non-membrane model was introduced to observe the influence on the drug release and gel erosion for surface area and shaking frequency.
方法采用无膜溶出模型，考察释放面积、振荡频率对眼用凝胶溶蚀及药物释放的影响。
Temperature-sensitive in situ gel, a kind of smart hydrogel, could be used as a good carrier for sustained, controlled and targeting drug release.
温敏在体凝胶作为一种智能水凝胶，可用作药物缓、控释和靶向输送的有效载体。
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